Canonical Allele Identifier: CA1619111269
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356194_31356230delinsTCTCCAGGTATCTGCGGAGCCACTCCACGCACTCGCC , CM000668.2:g.31356194_31356230delinsTCTCCAGGTATCTGCGGAGCCACTCCACGCACTCGCC GRCh38
NC_000006.11:g.31323971_31324007delinsTCTCCAGGTATCTGCGGAGCCACTCCACGCACTCGCC , CM000668.1:g.31323971_31324007delinsTCTCCAGGTATCTGCGGAGCCACTCCACGCACTCGCC GRCh37
NC_000006.10:g.31431950_31431986delinsTCTCCAGGTATCTGCGGAGCCACTCCACGCACTCGCC NCBI36
NG_023187.1:g.5983_6019delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2029_2065delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA
ENST00000481849.6:n.2029_2065delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA
ENST00000497377.6:n.2029_2065delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA
ENST00000640094.2:c.556_592delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA ENSP00000491275.2:p.Gly186=
ENST00000696558.1:c.556_592delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA ENSP00000512716.1:p.Gly186=
ENST00000696559.1:c.556_592delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA ENSP00000512717.1:p.Gly186=
ENST00000696560.1:c.556_592delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA ENSP00000512718.1:p.Gly186=
ENST00000696561.1:c.556_592delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA ENSP00000512719.1:p.Gly186=
ENST00000696562.1:c.556_592delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA ENSP00000512720.1:p.Gly186=
ENST00000412585.7:c.556_592delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA MANE Select ENSP00000399168.2:p.Gly186=
ENST00000412585.6:c.556_592delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA ENSP00000399168.2:p.Gly186=
ENST00000434333.1:c.589_625delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA ENSP00000405931.1:p.Gly197=
ENST00000474381.1:n.431_467delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA
ENST00000498007.1:n.822_858delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA
NM_005514.6:c.556_592delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA NP_005505.2:p.Gly186=
XM_011514556.1:c.589_625delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA XP_011512858.1:p.Gly197=
XM_011514557.1:c.556_592delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA XP_011512859.1:p.Gly186=
XR_926175.1:n.566_602delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA
NM_005514.7:c.556_592delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA NP_005505.2:p.Gly186=
NM_005514.8:c.556_592delinsGGCGAGTGCGTGGAGTGGCTCCGCAGATACCTGGAGA MANE Select NP_005505.2:p.Gly186=